, a light signaling responsive regulator, is involved in regulation of chaetoglobosin A biosynthesis and conidia development in .

Synth Syst Biotechnol

School of Life Science and Technology, Harbin Institute of Technology, No. 2 Yikuang Street, Nangang District, Harbin, 150080, People's Republic of China.

Published: December 2022

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Cytochalasans, with diverse structures and pharmacological activities, are a class of compounds containing isoindolinone moieties fused to the tricyclic or tetracyclic ring system. Chaetoglobosin A (cheA), mainly produced by , is the most abundant cytochalasan. However, limited understanding of transcriptional regulation of morphological development and cheA biosynthesis in has hindered cheA application in agriculture and biomedical field. This study examined the regulatory role of gene in . had significant effect on secondary metabolites production in , similar to that reported in other filamentous fungi. Inactivation of caused an obvious decrease in cheA production from 51.32 to 19.76 mg/L under dark conditions. In contrast, overexpression resulted in a dramatic increase in cheA production, reaching 206.59 mg/L under light conditions, which was higher than that noted under dark condition. The RT-qPCR results confirmed that as a light responsive regulator, positively regulated cheA biosynthesis by controlling the expression of core genes of the cheA biosynthetic gene cluster and other relevant regulators. Electrophoretic mobility shift assays proved that directly regulated , and , and indirectly regulated . Moreover, had a significant effect on the regulation of asexual spores production. When compared with wild-type , silenced and overexpression mutants presented remarkable differences in sporulation, irrespective of light or dark condition. Besides, expression was speculated to negatively regulate spore formation. These findings illustrated the regulatory mechanism of a hypothetical global regulator, in , suggesting its potential application in industrial-scale cheA biosynthesis.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356241PMC
http://dx.doi.org/10.1016/j.synbio.2022.07.002DOI Listing

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